ClearPoint Neuro Announces FDA Clearance and First-in-Human Cases Performed with the New 2.2 Software Version and the Integrated Maestro Brain Model
February 21 2024 - 4:05PM
ClearPoint Neuro, Inc. (Nasdaq: CLPT) (the “Company”), a global
device, cell, and gene therapy-enabling company offering precise
navigation to the brain and spine, today announced FDA Clearance
and first-in-human cases using the ClearPoint 2.2 Software with
integrated Maestro Brain Modeling, and also the publication of a
key validation study for its ClearPoint Maestro® Brain Model in the
peer-reviewed journal NeuroImage.1
“Leadership and innovation in any medical field requires not
only practical product development to deliver value for clinicians,
but also robust validation and peer review to show how and why
those products work,” commented Joe Burnett, President and CEO at
ClearPoint Neuro. “The Maestro Brain Model, and its integration
into the recently FDA cleared ClearPoint 2.2 navigation software,
is our latest example of just that. The ClearPoint system can now
offer fast, peri-procedural segmentation of the cortical structures
of the brain to identify both targets and safety zones for cell and
gene therapy delivery, laser ablation, biopsy and deep brain
stimulation. At the same time, we are pleased to announce that one
of many planned validation studies has been published online in the
journal NeuroImage to give surgeons confidence in the performance
and accuracy of the Maestro Tool. The first clinical cases using
ClearPoint 2.2 were completed successfully this quarter, and we
expect full market release in the second half of this year.”
MRI-guided neuro interventions require rapid, accurate, and
reproducible segmentation of anatomical brain structures for
identification of targets during surgical procedures. This
manuscript introduces the methodology for shape-constrained
deformable brain segmentation behind Maestro, describes the
validation performed for its FDA clearance, and presents a
comparison with manual expert segmentation and FreeSurfer, an
open-source segmentation software. Quantitative analysis indicates
superior performance compared to both manual expert segmentation
and FreeSurfer. The shape-constrained methodology results in
accurate and highly reproducible segmentation. Furthermore,
inherent point based-correspondence provides consistent target
identification ideal for MRI-guided neuro interventions. A link to
the open source publication can be found here.
Reproducibility error of Maestro (green),
FreeSurfer 7.2 (blue) and manual segmentation (red) for common
brain structures (left), and average over all structures (right).
Bars represent range of measured relative volume difference.
About ClearPoint Neuro
ClearPoint Neuro is a device, cell, and gene therapy-enabling
company offering precise navigation to the brain and spine. The
Company uniquely provides both established clinical products as
well as preclinical development services for controlled drug and
device delivery. The Company’s flagship product, the ClearPoint
Neuro Navigation System, has FDA clearance and is CE-marked.
ClearPoint Neuro is engaged with healthcare and research centers in
North America, Europe, Asia, and South America. The Company is also
partnered with the most innovative pharmaceutical/biotech
companies, academic centers, and contract research organizations,
providing solutions for direct CNS delivery of therapeutics in
pre-clinical studies and clinical trials worldwide. To date,
thousands of procedures have been performed and supported by the
Company’s field-based clinical specialist team, which offers
support and services to our customers and partners worldwide. For
more information, please visit www.clearpointneuro.com.
Forward-Looking Statements
This press release contains forward-looking statements within
the context of the federal securities laws, which may include the
Company’s expectation for the future market of its products and
services, and other performance and results. These forward-looking
statements are based on management’s current expectations and are
subject to the risks inherent in the business, which may cause the
Company's actual results to differ materially from those expressed
in or implied by forward-looking statements. Particular
uncertainties and risks include those relating to: global and
political instability, supply chain disruptions, labor shortages,
and macroeconomic and inflationary conditions; future revenue from
sales of the Company’s products and services; the Company’s ability
to market, commercialize and achieve broader market acceptance for
new products and services offered by the Company; the ability of
our biologics and drug delivery partners to achieve commercial
success, including their use of the Company’s products and services
in their delivery of therapies; the Company’s expectations,
projections and estimates regarding expenses, future revenue,
capital requirements, and the availability of and the need for
additional financing; the Company’s ability to obtain additional
funding to support its research and development programs; the
ability of the Company to manage the growth of its business; the
Company’s ability to attract and retain its key employees; and
risks inherent in the research, development, and regulatory
approval of new products. More detailed information on these and
additional factors that could affect the Company’s actual results
are described in the “Risk Factors” section of the Company’s Annual
Report on Form 10-K for the year ended December 31, 2022, and the
Company’s Quarterly Report on Form 10-Q for the three months ended
September 30, 2023, both of which have been filed with the
Securities and Exchange Commission, and the Company’s Annual Report
on Form 10-K for the year ended December 31, 2023, which the
Company intends to file with the Securities and Exchange Commission
on or before March 31, 2024. The Company does not assume any
obligation to update these forward-looking statements.
_____________________1 Zagorchev L, Hyde DE, Li C, et al.
Shape-constrained deformable brain segmentation: Methods and
quantitative validation. Neuroimage. Published online February 16,
2024. doi:10.1016/j.neuroimage.2024.120542
Photos accompanying this announcement are available at
https://www.globenewswire.com/NewsRoom/AttachmentNg/088f3809-a329-47e4-bfc0-21655bb9e1b2
https://www.globenewswire.com/NewsRoom/AttachmentNg/312932db-1574-4a9c-9bc4-5218308a2cee
Contact:
Media Contact:
Jacqueline Keller, Vice President of Marketing
(949) 900-6833
info@clearpointneuro.com
Investor Relations:
Danilo D’Alessandro, Chief Financial Officer
(888) 287-9109
ir@clearpointneuro.com
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